Institute of Experimental Medicine, Department of Genetics, Istanbul University, Istanbul, Turkey.
Dis Markers. 2010;28(6):353-60. doi: 10.3233/DMA-2010-0715.
The NOTCH signaling pathway plays important role in the development of multicellular organisms, as it regulates cell proliferation, survival, and differentiation. In adults, it is essential for the T- or B-lymphocyte lineage commitment. NOTCH1 and FBXW7 mutations both lead the activation of the NOTCH1 pathway and are found in the majority of T-ALL patients. In this study, the mutation analysis of NOTCH1 and FBXW7 genes was performed in 87 pediatric T-ALLs who were treated on the ALL-BFM protocols. In 19 patients (22%), activating NOTCH1 mutations were observed either in the heterodimerization domain or in the PEST domain and 7 cases (10%) demonstrated FBXW7 mutations (2 cases had both NOTCH1 and FBXW7 mutations). We also analyzed the relationship of the mutation data between the clinical and biological data of the patients. NOTCH1 and FBXW7, NOTCH1 alone were found correlated with lower initial leucocyte counts which was independent from the sex and T- cell immunophenotype. However, NOTCH1 and FBXW7 mutations were not predictive of outcome in the overall cohort of pediatric T-ALLs.
NOTCH 信号通路在多细胞生物的发育中起着重要作用,因为它调节细胞增殖、存活和分化。在成人中,它对于 T 或 B 淋巴细胞谱系的决定至关重要。NOTCH1 和 FBXW7 的突变都导致 NOTCH1 通路的激活,并且在大多数 T-ALL 患者中都可以发现。在这项研究中,对在 ALL-BFM 方案治疗的 87 例儿科 T-ALL 患者进行了 NOTCH1 和 FBXW7 基因突变分析。在 19 例患者(22%)中,观察到 NOTCH1 突变位于异二聚化结构域或 PEST 结构域,7 例(10%)显示 FBXW7 突变(2 例同时存在 NOTCH1 和 FBXW7 突变)。我们还分析了患者临床和生物学数据之间的突变数据之间的关系。NOTCH1 和 FBXW7、NOTCH1 单独与较低的初始白细胞计数相关,这与性别和 T 细胞免疫表型无关。然而,NOTCH1 和 FBXW7 突变不能预测儿科 T-ALL 患者的总体预后。